Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP315777.RAa_OMNsGccTdDVhEYBekx71Tae2zR5ojn2Ttg6u-J6Vk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP315777.RAa_OMNsGccTdDVhEYBekx71Tae2zR5ojn2Ttg6u-J6Vk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP315777.RAa_OMNsGccTdDVhEYBekx71Tae2zR5ojn2Ttg6u-J6Vk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP315777.RAa_OMNsGccTdDVhEYBekx71Tae2zR5ojn2Ttg6u-J6Vk130_provenance.
- NP315777.RAa_OMNsGccTdDVhEYBekx71Tae2zR5ojn2Ttg6u-J6Vk130_assertion description "[The aim of this study was to determine how often hematuria in families with TBMD segregated with haplotypes at the chromosomal loci for autosomal recessive and X-linked Alport syndrome (COL4A3/COL4A4 and COL4A5, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP315777.RAa_OMNsGccTdDVhEYBekx71Tae2zR5ojn2Ttg6u-J6Vk130_provenance.
- NP315777.RAa_OMNsGccTdDVhEYBekx71Tae2zR5ojn2Ttg6u-J6Vk130_assertion evidence source_evidence_literature NP315777.RAa_OMNsGccTdDVhEYBekx71Tae2zR5ojn2Ttg6u-J6Vk130_provenance.
- NP315777.RAa_OMNsGccTdDVhEYBekx71Tae2zR5ojn2Ttg6u-J6Vk130_assertion SIO_000772 11318937 NP315777.RAa_OMNsGccTdDVhEYBekx71Tae2zR5ojn2Ttg6u-J6Vk130_provenance.
- NP315777.RAa_OMNsGccTdDVhEYBekx71Tae2zR5ojn2Ttg6u-J6Vk130_assertion wasDerivedFrom befree-2016 NP315777.RAa_OMNsGccTdDVhEYBekx71Tae2zR5ojn2Ttg6u-J6Vk130_provenance.
- NP315777.RAa_OMNsGccTdDVhEYBekx71Tae2zR5ojn2Ttg6u-J6Vk130_assertion wasGeneratedBy ECO_0000203 NP315777.RAa_OMNsGccTdDVhEYBekx71Tae2zR5ojn2Ttg6u-J6Vk130_provenance.
- befree-2016 importedOn "2016-02-19" NP315777.RAa_OMNsGccTdDVhEYBekx71Tae2zR5ojn2Ttg6u-J6Vk130_provenance.